| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124422655-124422829 | Common:2; Rare:43 | ||||
| chr12:130871751-130872116 | Common:4; Rare:148 | ||||
| chr12:131710825-131711102 | Rare:66 | ||||
| chr12:132687295-132687651 | Common:2; Rare:134; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887558-132887763 | Rare:65 | ||||
| chr12:132956271-132956367 | Common:1; Rare:24 | ||||
| chr13:19633531-19633737 | Common:1; Rare:78 | ||||
| chr13:20525801-20525960 | Common:1; Rare:65 | ||||
| chr13:20773933-20774006 | Rare:25 | ||||
| chr13:21140194-21140636 | Rare:166 | ||||
| chr13:21176466-21176706 | Common:2; Rare:104 | ||||
| chr13:21459194-21459545 | Common:2; Rare:122 | ||||
| chr13:23889357-23889510 | Common:1; Rare:53 | ||||
| chr13:24160558-24160729 | Rare:47 | ||||
| chr13:24512728-24512870 | Common:3; Rare:41 |